TABLE 2.
Method | Site | Richnessa | Evennessb | Diversityc |
---|---|---|---|---|
LH-PCR | A | 20.0 ± 0.0cd | 0.91 ± 0.01b | 2.73 ± 0.02c |
B | 19.3 ± 0.5d | 0.90 ± 0.01c | 2.65 ± 0.04d | |
C1 | 22.0 ± 0.0b | 0.91 ± 0.01b | 2.80 ± 0.02b | |
C2 | 23.0 ± 0.0a | 0.92 ± 0.00a | 2.90 ± 0.01a | |
FAME | A | 34.0 ± 0.8a | 0.85 ± 0.00a | 3.00 ± 0.02a |
B | 30.5 ± 2.9b | 0.83 ± 0.02b | 2.82 ± 0.09b | |
C1 | 31.8 ± 1.0ab | 0.86 ± 0.00a | 2.96 ± 0.02a | |
C2 | 32.4 ± 1.0ab | 0.85 ± 0.01a | 2.96 ± 0.02a |
Richness is equal to the number of LH-PCR or FAME peaks.
Evenness is equal to diversity/ln (richness).
Diversity (Shannon index) (H) was calculated as follows: H = −Σpiln(pi), where pi is the relative abundance of a given LH-PCR or FAME peak.
Values are means ± standard deviations (n = 4). For each index, different letters indicate that values for different sites determined by the same method were significantly different (P < 0.05), as determined by one-way analysis of variance and least significant difference.